rs796053008

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs796053008(A;A)

Make rs796053008(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

165999776

Gene	LOC102724058, SCN1A

is a	snp
is	mentioned by
dbSNP	rs796053008
dbSNP (classic)	rs796053008
ClinGen	rs796053008
ebi	rs796053008
HLI	rs796053008
Exac	rs796053008
Gnomad	rs796053008
Varsome	rs796053008
LitVar	rs796053008
Map	rs796053008
PheGenI	rs796053008
Biobank	rs796053008
1000 genomes	rs796053008
hgdp	rs796053008
ensembl	rs796053008
geneview	rs796053008
scholar	rs796053008
google	rs796053008
pharmgkb	rs796053008
gwascentral	rs796053008
openSNP	rs796053008
23andMe	rs796053008
SNPshot	rs796053008
SNPdbe	rs796053008
MSV3d	rs796053008
GWAS Ctlg	rs796053008

Max Magnitude

0

ClinVar
Risk	rs796053008(A;A)
Alt	rs796053008(A;A)
Reference	Rs796053008(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	LOC102724058 SCN1A
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.166856286C>T
CLNSRC
CLNACC	RCV000188945.2,